NDC 72898-001 Dab
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Packages
NDC Code 72898-001-01
Package Description: 45 mL in 1 BOTTLE, PUMP
NDC Code 72898-001-02
Package Description: 250 mL in 1 BOTTLE, PUMP
NDC Code 72898-001-03
Package Description: 1200 mL in 1 BOTTLE, PUMP
NDC Code 72898-001-04
Package Description: 946352 mL in 1 DRUM
Product Details
What is NDC 72898-001?
What are the uses for Dab?
Which are Dab UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Dab Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- POLOXAMER 124 (UNII: 1S66E28KXA)
- D&C GREEN NO. 8 (UNII: I2W85YOX9L)
What is the NDC to RxNorm Crosswalk for Dab?
- RxCUI: 1046310 - benzalkonium chloride 0.12 % Topical Foam
- RxCUI: 1046310 - benzalkonium chloride 1.2 MG/ML Topical Foam
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".